In this article, we will explore the fascinating world of Bentazepam. From its origins to its relevance today, we will dive into the most important aspects of Bentazepam. We will analyze its impact on society, its evolution over time and possible future implications. Through a detailed and critical look, we will try to unravel the mysteries that surround Bentazepam, offering the reader a complete and enriching perspective on this topic.
Clinical data | |
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Trade names | Tiadipona (ES) |
AHFS/Drugs.com | International Drug Names |
Routes of administration | Oral (tablets) |
ATC code | |
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Pharmacokinetic data | |
Metabolism | Hepatic |
Elimination half-life | 2–4 hours |
Excretion | Renal |
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ChEMBL | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.123.659 |
Chemical and physical data | |
Formula | C17H16N2OS |
Molar mass | 296.39 g·mol−1 |
3D model (JSmol) | |
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Bentazepam (also known as Thiadipone, Tiadipona) is a thienodiazepine which is a benzodiazepine analog.
It possesses anxiolytic, anticonvulsant, sedative and skeletal muscle relaxant properties. Peak plasma rates are achieved in around 2,5 hours after oral administration. The elimination half-life is between approximately 2–4 hours. Bentazepam is effective as an anxiolytic.
A severe benzodiazepine overdose with bentazepam may result in coma and respiratory failure. Adverse effects include dry mouth, somnolence, asthenia, dyspepsia, constipation, nausea and drug-induced lymphocytic colitis has been associated with bentazepam. Severe liver damage and hepatitis has also been associated with bentazepam. Whilst liver failure from bentazepam is considered to be rare, liver function monitoring has been recommended for all patients taking bentazepam.